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<h2><b>Freelance Site Activation Specialist – Norway, Sweden or Denmark (Home-Based)</b></h2><p></p><p>Location: Norway, Sweden or Denmark (home-based)<br>Contract type: Freelance</p><p>FTE: 0.5 or 1.0<br>Start: immediately<br>Duration: around 4 month</p><p></p><p><b>About the Role</b></p><p>We are looking for a <b>Freelance Site Activation Specialist </b>based in Norway, Sweden or Denmark to support country-level clinical trial start-up and site management activities.</p><p>This role focuses on <b>feasibility, site identification, regulatory submissions, and activation</b>, with some involvement in maintenance activities. Candidates with <b>experience in all three countries</b> or exposure to the <b>Nordics region</b> are highly preferred.</p><p></p><h3><b>Key Responsibilities</b></h3><ul><li>Act as the primary point of contact for assigned investigative sites</li><li>Execute feasibility, site identification, and site activation activities in line with SOPs, regulations, and project timelines</li><li>Prepare, review, and manage essential site and regulatory documents, ensuring completeness and accuracy</li><li>Support contract and budget processes in collaboration with internal stakeholders</li><li>Maintain and update tracking tools, timelines, and internal systems with accurate project data</li><li>Monitor and report on site activation progress and performance metrics</li><li>Ensure compliance with ICH-GCP, local regulations (Germany and ideally Switzerland), and study requirements</li><li>Collaborate closely with Site Activation Managers, Project Management, and cross-functional teams</li></ul><p></p><h3><b>Requirements</b></h3><ul><li><b>Based in Norway, Denmark or Sweden</b> with strong understanding of the local regulatory environment</li><li><b>2–3+ years of experience</b> in site activation, study start-up, or clinical research</li><li>Bachelor’s degree in Life Sciences or related field</li><li>Solid knowledge of clinical trial start-up processes and regulatory requirements</li><li>Experience managing site documentation and submission processes</li><li>Strong attention to detail and ability to manage multiple sites and timelines</li><li><b>Fluent in Swedish, Norwegian or Danish and English (written and spoken)</b></li></ul><p></p><p></p><p>If this role sounds of interest, please apply today!</p><p></p><p>#LI-DNP</p><p>#LI-CES</p><p>#LI-HCPN</p><p>#LI-NS1</p><p></p><p>IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at <a href="https://jobs.iqvia.com/" target="_blank" rel="noopener noreferrer"><span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">https://jobs.iqvia.com</span></a></p><p></p><p>IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.</p><p></p>
